Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Diffuse tenosynovial giant cell tumor of first metatarsophalangeal joint |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Diffuse tenosynovial giant cell tumour of talonavicular joint |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Villonodular synovitis of ankle |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pigmented oral mucosal lesion |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Iron pigmentation of oral mucosa |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Exogenous pigmentation of oral mucosa |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Systemic exogenous pigmentation of oral mucosa |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Local exogenous pigmentation of oral mucosa |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Laugier-Hunziker syndrome |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Atrial myxoma with lentigines |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Genital lentiginosis |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Multiple lentigines syndrome |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Pigmentation of oral mucosa (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Lentigo maligna |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Exogenous ochronosis (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ochronosis due to homogentisate 1,2-dioxygenase deficiency (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ochronotic arthritis |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ocular albinism-lentigines-deafness syndrome |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Peutz-Jeghers polyps of small bowel |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Peutz-Jeghers syndrome |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
lentigo |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Lentiginosis |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital/hereditary lentiginosis |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Buccal pigmentation due to Addison's disease (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ochronosis caused by hydroquinone (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Nevoid lentiginosis |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Zosteriform lentiginosis (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Drug-induced oral pigmentation (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Villonodular synovitis of hip |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Villonodular synovitis of hip |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Villonodular synovitis of knee |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Villonodular synovitis of knee |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Villonodular synovitis of ankle |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Villonodular synovitis of ankle |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Diffuse tenosynovial giant cell tumour of talonavicular joint |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Diffuse tenosynovial giant cell tumour of talonavicular joint |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Diffuse tenosynovial giant cell tumor of first metatarsophalangeal joint |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Diffuse tenosynovial giant cell tumor of first metatarsophalangeal joint |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pigmented xerodermoid |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pigmented xerodermoid |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pigmented scar |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Mercury pigmentation of skin |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Carotene pigmentation of skin (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chrysoderma (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Conjunctival adrenochrome deposits (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Corneal pigmentation |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pigmentation of oral mucosa (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Conjunctival argyrosis |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, group F |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pigmented oral mucosal lesion |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Exogenous pigmentation of oral mucosa |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Local exogenous pigmentation of oral mucosa |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, group A |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Carotene pigmentation of skin (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Conjunctival pigmentation (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chlorpromazine pigmentation |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acquired anterior capsular pigmentation (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Mercury pigmentation of skin |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pigmented xerodermoid |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, group G |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Stromal corneal pigmentation |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chrysoderma (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Anterior corneal pigmentation |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, group D |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, group B |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Drug-induced oral pigmentation (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Progressive pigmentary dermatosis of Schamberg |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Buccal pigmentation due to Addison's disease (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Conjunctival adrenochrome deposits (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ochronotic arthritis |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Laugier-Hunziker syndrome |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Corneal pigmentation |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Non-neurologic xeroderma pigmentosum |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, group C (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, group E (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, variant form |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Iron pigmentation of oral mucosa |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Systemic exogenous pigmentation of oral mucosa |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Meconium pigmentation (morphologic abnormality) |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Amalgam tattoo |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Local exogenous pigmentation of oral soft tissue |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chlorpromazine pigmentation |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Drug-induced oral pigmentation (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Conjunctival adrenochrome deposits (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
ictère périnatal causé par une hémolyse excessive |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, group B |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Non-neurologic xeroderma pigmentosum |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Pigmented xerodermoid |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Xeroderma pigmentosum, group C (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Xeroderma pigmentosum, group G |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Xeroderma pigmentosum, group F |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Xeroderma pigmentosum, group A |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Xeroderma pigmentosum (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Xeroderma pigmentosum, group E (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Xeroderma pigmentosum, group D |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Xeroderma pigmentosum, variant form |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Xeroderma pigmentosum/Cockayne syndrome complex (XP/CS complex) is characterized by the cutaneous features of xeroderma pigmentosum (XP) together with the systemic and neurological features of Cockayne syndrome. |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Pigment dispersion syndrome of bilateral eyes (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pigment dispersion syndrome of bilateral eyes (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |